Our Prenatal Diagnosis helps at-risk couples detect their baby’s genotype early. Over 3,568 have benefited.
Our Prenatal Diagnosis (PND) Unit provides highly specialised genetic testing services to support the prevention and management of sickle cell disorder and other inherited conditions. As one of the Foundation's flagship services, PND enables expectant parents to determine the haemoglobin genotype of their unborn child early in pregnancy. The unit also offers fetal gender determination and twin relationship testing to identify whether twins are identical or fraternal.
Early diagnosis empowers families with accurate information to make timely, informed decisions during pregnancy. Our laboratory tests for a range of fetal haemoglobin genotypes, including HbA, HbAS, HbS, HbC, HbD, and HbG. With results delivered within just three working days, we provide one of the fastest turnaround times, ensuring families receive the answers they need without unnecessary delays.
Our Prenatal Diagnosis Unit continues to set the standard for excellence in genetic testing and counselling. To date, we have successfully carried out over 3,568 Prenatal Diagnosis procedures with a 99% success rate, helping thousands of families make informed choices with confidence.
